Whole-Exome Sequencing Reveals GATA4 and PTEN Mutations as a Potential Digenic Cause of Left Ventricular Noncompaction-Reference-Cited by-同舟云学术

Whole-Exome Sequencing Reveals GATA4 and PTEN Mutations as a Potential Digenic Cause of Left Ventricular Noncompaction

Published:2018-01 Issue:1 Volume:11 Page:
ISSN:2574-8300
Container-title:Circulation: Genomic and Precision Medicine
language:en
Short-container-title:Circ: Genomic and Precision Medicine

Author:

Tang Vi T.¹,Arscott Patricia¹,Helms Adam S.¹,Day Sharlene M.¹

Affiliation:

1. From the Departments of Molecular and Integrative Physiology (V.T.T., S.M.D.) and Internal Medicine (P.A., A.S.H., S.M.D.), University of Michigan, Ann Arbor.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference29 articles.

1. PKG-1α mediates GATA4 transcriptional activity

2. Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers

3. Ontogeny of phosphoinositide 3-kinase signaling in developing heart: effect of acute β-adrenergic stimulation

4. PTENhamartoma tumor syndrome and Gorham-Stout phenomenon

5. Phosphoinositide-3 Kinase Signaling in Cardiac Hypertrophy and Heart Failure

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